- This topic has 1 reply, 1 voice, and was last updated 10 years ago by .
- You must be logged in to reply to this topic.
Dr. Diana, both a doctor (therapeutic optometrist), and a recovered POTS and ME/CFS patient, offers help and hope for POTS, Dysautonomia, Ehlers-Danlos syndrome, Chronic Fatigue, Chronic Lyme, vascular abnormalities, Fibromyalgia, and Multiple Sclerosis. Dr. Diana is now working full time at POTS Care.
NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › Who is the right specialty to see for EDS diagnosis?
My son is interested in being tested for EDS. He already went through genetic testing for Marfan Syndrome and didn’t have “enough” symptoms for a positive diagnosis; however, he seems to fall into the possibility of EDS. I’m just curious, who would be the right speciality to be sent to for appropriate testing? We had Kaiser before, and now we don’t. We have Private Ins.
Thank you! I didn’t think about that! Duh, me!
This website was created to inform, educate and brainstorm with fellow patients and doctors. The content should not be used as a substitute for professional medical advice, diagnosis or treatment. Readers are encouraged to confirm all information with other sources and their physicians. The creator of this site will not be liable for any direct, indirect, consequential, special, exemplary, or other damages arising from the use of this website.
Twitter: @prettyill
“Dr. Diana will always hold a very special place in my heart for her selfless devotion to helping everyone, not just the Ehlers-Danlos community. I hate to think what my life would be without her insight and guidance.”
-- Chris Gross